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D

David Curtis

University of London

73H指数
525论文数
5.5W被引数
收录论文 115
发表时间
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Exome-wide association study of suicidal ideation and behaviour has unclear implications全外显子组关联研究对自杀意念和行为的影响尚不明确
errJournal of Affective Disorders
IF4.9
err2025-11-15
err0
PREAI
errDavid Curtis
err分享
err收藏
Health effects of loss of function variants in gene targets for Alzheimer’s disease prevention阿尔茨海默病预防靶基因中功能缺失变异的健康影响
errNeurological Sciences
IF2.4
err2025-10-22
err0
errOAAI
errYuan Ma; Allena Zhang; Sabrina Asri; David Curtis
err分享
err收藏
Analysis of whole genome sequence data shows association of Alzheimer's disease with rare coding variants in ABCA7, PSEN1, SORL1 and TREM2全基因组序列数据分析显示，阿尔茨海默病与ABCA7、PSEN1、SORL1和TREM2基因中的罕见编码变异存在关联。
errJOURNAL OF NEUROGENETICS
IF2
err2025-09-01
err0
PREAI
errCurtis, David; Joseph, Shujaani
err分享
err收藏
Assessment of ability of a DNA language model to predict pathogenicity of rare coding variants评估DNA语言模型预测稀有编码变异致病性的能力
errJournal of Human Genetics
IF2.5
err2025-08-15
err0
errOAAI
errDavid Curtis
err分享
err收藏
Analysis of 470,000 exome-sequenced cases and controls fails to identify any genes impacting risk of developing affective disorder对47万例外显子测序病例和对照的研究未能识别出任何影响情感障碍发病风险基因。
errACTA NEUROPSYCHIATRICA
IF2.5
err2025-06-30
err2
errOAAI
errCurtis, David
err分享
err收藏
Analysis of rare coding variants in 470,000 exome-sequenced subjects characterises contributions to risk of type 2 diabetes对470,000例外显子测序样本中的罕见编码变异进行分析，可表征其对2型糖尿病风险的贡献。
errPLOS ONE
IF2.6
err2024-12-12
err0
errOAAI
errCurtis, D
err分享
err收藏
Assessment of ability of AlphaMissense to identify variants affecting susceptibility to common disease
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-08-03
err2
errOAAI
errCurtis, David
err分享
err收藏
Genetic Variants Associated with Hypertension Risk: Progress and Implications
errPULSE
IF7.3
err2024-01-27
err1
errOAAI
errCurtis, David
err分享
err收藏
Editorial: Glutamatergic system in affective and psychotic disorders: pre-clinical and clinical advances
errFRONTIERS IN NEUROSCIENCE
IF3.2
err2024-01-09
err0
errOAAI
errStrzelecki, Dominik; Talarowska, Monika; Kazmierski, Jakub; Waszkiewicz, Napoleon; Curtis, David
err分享
err收藏
Analysis of rare variants in 470,000 exome-sequenced UK Biobank participants implicates novel genes affecting risk of hypertension
errPULSE
IF7.3
err2023-11-13
err3
errOAAI
errCurtis, David
err分享
err收藏
Social scientists would do well to steer clear of polygenic scores
errBEHAVIORAL AND BRAIN SCIENCES
IF13.7
err2023-09-11
err1
errOAAI
errCurtis, David
err分享
err收藏
The human genome harbours widespread exclusive yin yang haplotypes
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2023-06-12
err3
errOAAI
errCurtis, David; Amos, William
err分享
err收藏
RE: Extending the vulnerability-stress model of mental disorders: three-dimensional NPSR1 x environment x coping interaction study in anxiety
errBRITISH JOURNAL OF PSYCHIATRY
IF7.6
err2022-12-19
err0
errOAAI
errCurtis, David
err分享
err收藏
Concerns about the use of polygenic embryo screening for psychiatric and cognitive traits
errLANCET PSYCHIATRY
IF24.8
err2022-10-01
err16
errOAAI
errLencz, Todd; Sabatello, Maya; Docherty, Anna; Peterson, Roseann E.; Soda, Takahiro; Austin, Jehannine; Bierut, Laura; Crepaz-Keay, David; Curtis, David; Degenhardt, Franziska; Huckins, Laura; Lazaro-Munoz, Gabriel; Mattheisen, Manuel; Meiser, Bettina; Peay, Holly; Rietschel, Marcella; Walss-Bass, Consuelo; Davis, Lea K.
err分享
err收藏
Comment on Evaluation of a Gene-Environment Interactionof PON1 and Low-Level Nerve Agent Exposure with Gulf WarIllness: A Prevalence Case-Control Study Drawn from the US Military Health Survey's National Population Sample
errENVIRONMENTAL HEALTH PERSPECTIVES
IF9.8
err2022-06-01
err2
errOAAI
errCurtis, David
err分享
err收藏
Identification of specific genes involved in schizophrenia aetiology - what difference does it make? (Apr, pg 1, 2022)
errBRITISH JOURNAL OF PSYCHIATRY
IF7.6
err2022-05-23
err0
errOAAI
errCurtis, David
err分享
err收藏
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia双相情感障碍中的外显子组测序将AKAP11鉴定为与精神分裂症共享的风险基因
errNATURE GENETICS
IF31.8
err2022-04-11
err70
errOAAI
errPalmer, Duncan S.; Howrigan, Daniel P.; Chapman, Sinead B.; Adolfsson, Rolf; Bass, Nick; Blackwood, Douglas; Boks, Marco P. M.; Chen, Chia-Yen; Churchhouse, Claire; Corvin, Aiden P.; Craddock, Nicholas; Curtis, David; Di Florio, Arianna; Dickerson, Faith; Freimer, Nelson B.; Goes, Fernando S.; Jia, Xiaoming; Jones, Ian; Jones, Lisa; Jonsson, Lina; Kahn, Rene S.; Landen, Mikael; Locke, Adam E.; McIntosh, Andrew M.; McQuillin, Andrew; Morris, Derek W.; O'Donovan, Michael C.; Ophoff, Roel A.; Owen, Michael J.; Pedersen, Nancy L.; Posthuma, Danielle; Reif, Andreas; Risch, Neil; Schaefer, Catherine; Scott, Laura; Singh, Tarjinder; Smoller, Jordan W.; Solomonson, Matthew; St Clair, David; Stahl, Eli A.; Vreeker, Annabel; Walters, James T. R.; Wang, Weiqing; Watts, Nicholas A.; Yolken, Robert; Zandi, Peter P.; Neale, Benjamin M.
err分享
err收藏
Identification of specific genes involved in schizophrenia aetiology - what difference does it make?
errBRITISH JOURNAL OF PSYCHIATRY
IF7.6
err2022-04-06
err2
errOAAI
errCurtis, David
err分享
err收藏
Should all babies have their genome sequenced at birth?
errBMJ-BRITISH MEDICAL JOURNAL
IF42.7
err2021-11-17
err18
errOAAI
errBiesecker, Leslie G.; Green, Eric D.; Manolio, Teri; Solomon, Benjamin D.; Curtis, David
err分享
err收藏
Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension
errPULSE
IF7.3
err2021-07-05
err11
errOAAI
errCurtis, David
err分享
err收藏

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